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Ambulans Ked Rescue Vest

by Ambulans İlkyardim Ve Hastahane Ci̇hazlari Ve Tesi̇sleri̇ San. Ti̇c.a.ş.

Ref AKY-1Model AMBULANS KED KURTARMA YELEĞİ

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number869760343AKKY-1ND Basic UDI-DI 08697603430550UDI-DIDate13 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
AMBULANS KED KURTARMA YELEĞİ, AKY-1
Primary DI / UDI-DI
08697603430550
Basic UDI-DI
869760343AKKY-1ND
Direct Marketing DI
08697603430550
EMDN Code
V08050103, V0805038002
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018558

Other devices from Ambulans İlkyardim Ve Hastahane Ci̇hazlari Ve Tesi̇sleri̇ San. Ti̇c.a.ş.

See all devices from Ambulans İlkyardim Ve Hastahane Ci̇hazlari Ve Tesi̇sleri̇ San. Ti̇c.a.ş. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No